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窄带311纳米紫外线B辐射引发的抗氧化反应与宽带紫外线不同。

Narrow-Band 311 nm Ultraviolet-B Radiation Evokes Different Antioxidant Responses from Broad-Band Ultraviolet.

作者信息

Rácz Arnold, Hideg Éva

机构信息

Department of Plant Biology, University of Pécs, Ifjúság útja 6, 7624 Pécs, Hungary.

出版信息

Plants (Basel). 2021 Jul 30;10(8):1570. doi: 10.3390/plants10081570.

Abstract

Supplemental narrow-band 311 nm UV-B radiation was applied in order to study the effect of this specific wavelength on tobacco as a model plant. UV-B at photon fluxes varying between 2.9 and 9.9 μmol m s was applied to supplement 150 μmol m s photosynthetically active radiation (PAR) for four hours in the middle of the light period for four days. Narrow-band UV-B increased leaf flavonoid and phenolic acid contents. In leaves exposed to 311 nm radiation, superoxide dismutase activity increased, but phenolic peroxidase activity decreased, and the changes were proportional to the UV flux. Ascorbate peroxidase activities were not significantly affected. Narrow-band UV-B caused a dose-dependent linear decrease in the quantum efficiency of photosystem II, up to approximately 10% loss. A parallel decrease in non-regulated non-photochemical quenching indicates potential electron transfer to oxygen in UV-treated leaves. In addition to a flux-dependent increase in the imbalance between enzymatic HO production and neutralization, this resulted in an approximately 50% increase in leaf HO content under 2.9-6 μmol m s UV-B. Leaf HO decreased to control levels under higher UV-B fluxes due to the onset of increased non-enzymatic HO- and superoxide-neutralizing capacities, which were not observed under lower fluxes. These antioxidant responses to 311 nm UV-B were different from our previous findings in plants exposed to broad-band UV-B. The results suggest that signaling pathways activated by 311 nm radiation are distinct from those stimulated by other wavelengths and support the heterogeneous regulation of plant UV responses.

摘要

为了研究这种特定波长对作为模式植物的烟草的影响,施加了补充窄带311 nm UV-B辐射。在光照期的中间时段,以2.9至9.9 μmol m⁻² s⁻¹之间变化的光子通量施加UV-B,以补充150 μmol m⁻² s⁻¹的光合有效辐射(PAR),持续四天,每天四小时。窄带UV-B增加了叶片类黄酮和酚酸含量。在暴露于311 nm辐射的叶片中,超氧化物歧化酶活性增加,但酚类过氧化物酶活性降低,且这些变化与UV通量成正比。抗坏血酸过氧化物酶活性未受到显著影响。窄带UV-B导致光系统II的量子效率呈剂量依赖性线性下降,损失高达约10%。非调节性非光化学猝灭的平行下降表明在UV处理的叶片中存在潜在的电子向氧的转移。除了酶促产生的HO与中和之间的不平衡随通量增加外,这还导致在2.9 - 6 μmol m⁻² s⁻¹的UV-B处理下叶片HO含量增加约50%。在较高的UV-B通量下,由于非酶促HO和超氧化物中和能力增加的开始,叶片HO降至对照水平,而在较低通量下未观察到这种情况。这些对311 nm UV-B的抗氧化反应与我们之前在暴露于宽带UV-B的植物中的发现不同。结果表明,由311 nm辐射激活的信号通路与其他波长刺激的信号通路不同,并支持植物UV反应的异质性调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/750b/8400681/d38a6b3e2231/plants-10-01570-g001.jpg

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